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神经纤毛蛋白:C末端规则肽及其与伤害感受和COVID-19的关联。

Neuropilins: C-end rule peptides and their association with nociception and COVID-19.

作者信息

Jobe Amie, Vijayan Ranjit

机构信息

Department of Biology, College of Science, United Arab Emirates University, PO Box 15551, Al Ain, United Arab Emirates.

出版信息

Comput Struct Biotechnol J. 2021;19:1889-1895. doi: 10.1016/j.csbj.2021.03.025. Epub 2021 Mar 26.

Abstract

Viral internalization is aided by host cell surface receptors. In the case of SARS-CoV-2 and SARS-CoV, the primary host receptor is the angiotensin-converting enzyme 2 (ACE2). Considering the disparities in the transmission rate and viral tropism of the two coronaviruses, additional host factors were suspected. Recently, a novel host factor for SARS-CoV-2 entry, neuropilin-1 (NRP-1) has been identified. These receptors potentiate viral infection in the presence of other host factors like ACE2. Through its C-end rule (CendR) motif exposed following furin processing, the SARS-CoV-2 spike protein binds to the CendR pocket of NRP-1 and achieves cell entry through endocytosis. The binding of SARS-CoV-2 spike protein to the NRP-1 receptor interferes with the docking of its endogenous ligand VEGF-A, signaling that would otherwise promote nociception. This review looks at the function of neuropilins and how it contributes to SARS-CoV-2 infection and nociception.

摘要

病毒内化借助宿主细胞表面受体。就严重急性呼吸综合征冠状病毒2(SARS-CoV-2)和严重急性呼吸综合征冠状病毒(SARS-CoV)而言,主要的宿主受体是血管紧张素转换酶2(ACE2)。鉴于这两种冠状病毒在传播率和病毒嗜性方面存在差异,人们怀疑还有其他宿主因子。最近,一种用于SARS-CoV-2进入的新型宿主因子——神经纤毛蛋白1(NRP-1)已被确定。在诸如ACE2等其他宿主因子存在的情况下,这些受体可增强病毒感染。严重急性呼吸综合征冠状病毒2刺突蛋白经弗林蛋白酶加工后暴露其C端规则(CendR)基序,该蛋白与神经纤毛蛋白1的CendR口袋结合,并通过内吞作用实现细胞进入。严重急性呼吸综合征冠状病毒2刺突蛋白与神经纤毛蛋白1受体的结合会干扰其内源性配体血管内皮生长因子A(VEGF-A)的对接,而该信号传导原本会促进伤害感受。本综述探讨了神经纤毛蛋白的功能及其如何促成严重急性呼吸综合征冠状病毒2感染和伤害感受。

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